岗位职责：

1. Be respoible for realizing registration objectives as the scheduled

2. Resolving the problems occurred during the registration process by communicating and/or negotiating with the spoor.

3. Building and keeping good relatiohip with regulatory authorities.

4. Be respoible for CE mark for EHZP local products, including IEC/EMChipping testing and prepare TF.

1. 按公司计划，基本能够独立完成产品的注册任务；

2. 对于注册过程中遇到的问题能主动通过良好的多方沟通予以解决；

3. 与药监局及检测机构等保持良好的沟通；

4. 协助完成注册临床试验项目,从项目启动到临床试验总结报告的完成。

任职要求：

1. Bachelor degree or above of medicine & pharmaceutical, biology or related area

2. At least 1 year working experience of product registration.

3. Practiced skills on computer, master in oral and written English

4. Good communication and coordination skill

5. Good organization and planning skill

1. 本科以上(含)学历，生物或医药相关专业；

2. 具有1-2 年的医疗器械和体外诊断试剂类产品的注册经验；

3. 学习能力强，有责任感；

4. 良好的沟通能力并能和不同层级的人很好的相处；

5. 良好的组织和计划能力

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